NCT07154017

Brief Summary

The objective of this study will be to determine whether the combination of movement imaging techniques with neural mobilization (NM) exercises works to modify median nerve sensitivity to mechanical stimuli. Movement Representation Techniques (MRTs) are defined as therapeutic or training systems that neurophysiologically evoke a perceptual-cognitive representation of movement. They can be combined with the execution of actual movement or with afferent sensory stimulation (motor command). There is evidence demonstrating positive results in pain reduction and improved range of motion using MRTs alone. The study will be evaluated in 10 randomly selected asymptomatic volunteers, considering the following variables: pressure pain threshold, elbow extensor range of motion, and sensory responses before and after the intervention, in both the experimental and control groups. The period between interventions will be 72 hours.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 18, 2025

Completed
14 days until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 4, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

September 4, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

August 18, 2025

Last Update Submit

August 26, 2025

Conditions

Keywords

Movement Representation TechniquesNeural MobilizationMechanosensitivity

Outcome Measures

Primary Outcomes (3)

  • Elbow Extensor Range of Motion

    The elbow extension movement will be measured during the median nerve provocation test, through digital inclinometry of both the dominant and non-dominant arm by an experienced Physiotherapist.

    Pre- and post-interventions with a 72-hour washout period, for both control and experimental.

  • Pressure Pain Threshold

    Pressure pain thresholds (PPTs) will be performed at two sites, the dominant and non-dominant side, in asymptomatic participants: 1) the upper trapezius muscle, and 2) the proximal third of the forearm. A pressure algometer will be used. The device has a rod at one end with a 1 cm2 flat, circular rubber tip. Pressure will be applied progressively in a perpendicular direction at a rate of 0.5 kgf/cm2 per second to the assessment sites. Volunteers will be asked to verbally report the moment they feel the pressure exerted with the pressure algometer begin to change to a sensation of pain (first painful sensation). At that moment, the evaluator will stop applying pressure and a value will be obtained. Three measurements will be taken at each site, 30 seconds apart. The PPT will be determined as the arithmetic mean of the three measurements.

    Pre and post interventions, both control and experimentalPre- and post-interventions with a 72-hour washout period, for both control and experimental.

  • Spatiotemporal distribution of sensory responses

    Humanoid software (University Center of Assistance, Teaching and Investigation, CUADI, Argentina) will be used to evaluate the spatiotemporal distribution of pain intensity and/or perceived sensations. To mark the sensations that subject feel during the arm stretch test. To do this, the subjects will mark the area on the touchscreen where they perceive tension or stretching. The sensations will be representated by different colours: yellow is used for mild sensations, orange for moderate sensations, and red for intense sensations.

    Pre- and post-interventions with a 72-hour washout period, for both control and experimental.

Study Arms (2)

Combination of Movement Representation Techniques with Neural Mobilization Exercises (experimental)

EXPERIMENTAL

Combination of Movement Representation Techniques (Action observation, Motor imagery and Mirror therapy) with Neural Mobilization Exercises (Active neural mobilization of Median nerve)

Other: Combination of Movement Representation Techniques with neural mobilization exercises

Neural Mobilization Excercises (control)

ACTIVE COMPARATOR

Neural Mobilization Exercises (Active neural mobilization of Median nerve)

Other: Neural mobilization exercises

Interventions

The experimental intervention will be an exposition of movement representation techniques in an established sequential order, consisting of action observation, implicit/explicit motor imagery and visual feedback with a mirror in combination with neural mobilization exercises.

Combination of Movement Representation Techniques with Neural Mobilization Exercises (experimental)

The control intervention will consist in three series of active neural mobilization exercises

Also known as: Neurodinamics excercises
Neural Mobilization Excercises (control)

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • asymptomatic volunteers of both sexes
  • aged 18 to 45
  • with no symptoms or history of disease in the cervical region, shoulder girdle, or upper limb.

You may not qualify if:

  • history of surgery or trauma to the cervical spine, shoulder girdle, or upper limb;
  • nonspecific shoulder pain;
  • presenting symptoms of chronic pain in any region of the body;
  • aphantasia (inability to create mental images);
  • hypermobility;
  • history of cancer or active disease;
  • current infection;
  • rheumatological disease;
  • neurological and/or psychiatric disorders;
  • altered sensation;
  • current pregnancy;
  • consumption of centrally acting medications;
  • undergoing physiotherapy treatment in the last month;
  • inability to understand the informed consent document;
  • previous experience with median nerve provocation testing.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Gran Rosario

Rosario, Santa Fe Province, 2000, Argentina

Location

Related Publications (1)

  • Matesanz-Garcia L, Caceres-Pajuelo JE, Cuenca-Martinez F, La Touche R, Goicoechea-Garcia C, Fernandez-Carnero J. Effects of neural mobilizations through movement representation techniques for the improvement of neural mechanosensitivity of the median nerve region: a randomized controlled trial. Somatosens Mot Res. 2021 Dec;38(4):267-276. doi: 10.1080/08990220.2021.1964463. Epub 2021 Aug 17.

Central Study Contacts

Maximiliano Venosta, Physiotherapist

CONTACT

Mauro S Barone, Doctor-Physiotherapist

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
Evaluators
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: A Pilot Study, Single-blind,Randomized, Crossover.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physioterapist

Study Record Dates

First Submitted

August 18, 2025

First Posted

September 4, 2025

Study Start

September 1, 2025

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

September 4, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will share

Yes, the statistical analysis and consent form

Shared Documents
SAP, ICF
Time Frame
From first date of publication of journal article.
Access Criteria
IPD will be provided upon request.

Locations